BRPI1006812A8 - n- (4 - {[6,7-bis (methyloxy) quinolin-4-yl] phenyl) -N- (4-fluorophenyl) cyclopropane-1,1-dicarboxamide malate salt - Google Patents

n- (4 - {[6,7-bis (methyloxy) quinolin-4-yl] phenyl) -N- (4-fluorophenyl) cyclopropane-1,1-dicarboxamide malate salt Download PDF

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Publication number
BRPI1006812A8
BRPI1006812A8 BRPI1006812A BRPI1006812A BRPI1006812A8 BR PI1006812 A8 BRPI1006812 A8 BR PI1006812A8 BR PI1006812 A BRPI1006812 A BR PI1006812A BR PI1006812 A BRPI1006812 A BR PI1006812A BR PI1006812 A8 BRPI1006812 A8 BR PI1006812A8
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Brazil
Prior art keywords
phenyl
methyloxy
quinolin
bis
cyclopropane
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BRPI1006812A
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Portuguese (pt)
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Adrian St Clair Brown
William P Gallagher
Peter Lamb
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Exelixis Inc
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Application filed by Exelixis Inc filed Critical Exelixis Inc
Publication of BRPI1006812A2 publication Critical patent/BRPI1006812A2/en
Publication of BRPI1006812A8 publication Critical patent/BRPI1006812A8/en
Publication of BRPI1006812B1 publication Critical patent/BRPI1006812B1/en
Publication of BRPI1006812B8 publication Critical patent/BRPI1006812B8/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/14Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/233Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Diabetes (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Quinoline Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

sais de malato de n-(4-{[6,7-bis(metiloxi)quinolin-4- il]oxi}fenil)-n'-(4-flúor fenil)ciclopropan0-1,1- dicarboxamida, e formas cristalinas destes o revelado são sais de mala to de n- ( 4- { [ 6, 7- bis(metiloxi)-quinolin-4-il]oxi}fenil)-n'-(4-flúor fenil)ciclopropano-1,1-dicarboxamida, incluindo um (l)-sal de malato, um (d)-sal de malato, um (dl) sal de malato, e misturas destes; e formas cristalinas e formas amorfas dos sais de malato. também revelado são composições farmacêuticas compreendendo pelo menos um sal de malato de n-(4-{ [6,7-bis(metiloxi)quinolin-4-il]oxi}fenil)-n'-(4- flúor fenil) -ciclopropano-1, 1-dicarboxamida; e métodos de tratamento de câncer compreendendo administrar pelo menos um sal de malato de n-(4-{ [6,7-bis(metiloxi)quinolin-4- il]oxi}fenil)-n'-(4-flúorfenil)ciclopropano-1,1- dicarboxamida.n- (4 - {[6,7-bis (methyloxy) quinolin-4-yl] oxy} phenyl) -N '- (4-fluoro phenyl) cyclopropan0-1,1-dicarboxamide malate salts, and crystalline forms of these disclosed are n- (4 - {[6,7-bis (methyloxy) quinolin-4-yl] oxy} phenyl) -N '- (4-fluorine phenyl) cyclopropane-1,1-malate salts. dicarboxamide, including one (1) malate salt, one (d) malate salt, one (dl) malate salt, and mixtures thereof; and crystalline forms and amorphous forms of the malate salts. Also disclosed are pharmaceutical compositions comprising at least one n- (4 - {[6,7-bis (methyloxy) quinolin-4-yl] oxy} phenyl) -N '- (4-fluoro phenyl) cyclopropane malate salt -1,1-dicarboxamide; and cancer treatment methods comprising administering at least one n- (4- {[6,7-bis (methyloxy) quinolin-4-yl] oxy} phenyl) -n '- (4-fluorophenyl) cyclopropane malate salt -1,1-dicarboxamide.

BRPI1006812A 2009-01-16 2010-01-15 L-MALATE CRYSTALLINE FORM OF N-(4-{[6,7-BIS(METYLOXY)-QUINOLIN-4-YL]OXY}PHENYL)-N'-(4-FLUORPHENYL)CYCLOPROPANE-1,1-DICARBOXAMIDE, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF BRPI1006812B8 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US14542109P 2009-01-16 2009-01-16
US61/145,421 2009-01-16
PCT/US2010/021194 WO2010083414A1 (en) 2009-01-16 2010-01-15 Malate salt of n- (4- { [ 6, 7-bis (methyloxy) quin0lin-4-yl] oxy}phenyl-n' - (4 -fluorophenyl) cyclopropane-1-dicarboxamide, and crystalline forms therof for the treatment of cancer

Publications (4)

Publication Number Publication Date
BRPI1006812A2 BRPI1006812A2 (en) 2019-07-09
BRPI1006812A8 true BRPI1006812A8 (en) 2019-08-06
BRPI1006812B1 BRPI1006812B1 (en) 2022-12-06
BRPI1006812B8 BRPI1006812B8 (en) 2023-01-24

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ID=41820137

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI1006812A BRPI1006812B8 (en) 2009-01-16 2010-01-15 L-MALATE CRYSTALLINE FORM OF N-(4-{[6,7-BIS(METYLOXY)-QUINOLIN-4-YL]OXY}PHENYL)-N'-(4-FLUORPHENYL)CYCLOPROPANE-1,1-DICARBOXAMIDE, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

Country Status (25)

Country Link
US (12) US8877776B2 (en)
EP (1) EP2387563B2 (en)
JP (6) JP5677318B2 (en)
KR (8) KR20230008268A (en)
CN (3) CN106083714B (en)
AR (1) AR075025A1 (en)
AU (3) AU2010204619B2 (en)
BR (1) BRPI1006812B8 (en)
CA (2) CA2758030C (en)
DK (1) DK2387563T4 (en)
EA (3) EA019959B1 (en)
ES (1) ES2402524T5 (en)
HK (1) HK1164305A1 (en)
HR (1) HRP20130458T4 (en)
IL (2) IL214086A (en)
MX (3) MX2011007620A (en)
NZ (3) NZ779754A (en)
PL (1) PL2387563T5 (en)
PT (1) PT2387563E (en)
RS (1) RS52754B2 (en)
SG (1) SG173014A1 (en)
SM (1) SMT201300050B (en)
TW (7) TWI577664B (en)
WO (1) WO2010083414A1 (en)
ZA (1) ZA201105167B (en)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4638436B2 (en) 2003-09-26 2011-02-23 エグゼリクシス, インコーポレイテッド c-Met modulators and uses thereof
TWI577664B (en) * 2009-01-16 2017-04-11 艾克塞里克斯公司 Malate salt of n-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, pharmaceutical composition comprising the same and use thereof
UA108618C2 (en) * 2009-08-07 2015-05-25 APPLICATION OF C-MET-MODULATORS IN COMBINATION WITH THEMOSOLOMID AND / OR RADIATION THERAPY FOR CANCER TREATMENT
US20120070368A1 (en) * 2010-04-16 2012-03-22 Exelixis, Inc. Methods of Using C-Met Modulators
US9724342B2 (en) * 2010-07-16 2017-08-08 Exelixis, Inc. C-met modulator pharmaceutical compositions
KR101882328B1 (en) * 2010-09-27 2018-07-27 엑셀리시스, 인코포레이티드 Dual inhibitors of met and vegf for the treatment of castration-resistant prostate cancer and osteoblastic bone metastases
US9717720B2 (en) * 2011-02-10 2017-08-01 Exelixis, Inc. Processes for preparing quinoline compounds and pharmaceutical compositions containing such compounds
US20120252840A1 (en) 2011-04-04 2012-10-04 Exelixis, Inc. Method of Treating Cancer
BR212013028314U2 (en) 2011-05-02 2015-11-03 Exelixis Inc Method to Treat Cancer and Bone Cancer Pain
CA2848512A1 (en) 2011-09-22 2013-03-28 Exelixis, Inc. Method for treating osteoporosis
WO2013059788A1 (en) * 2011-10-20 2013-04-25 Exelixis, Inc. Process for preparing quinoline derivatives
WO2013166296A1 (en) 2012-05-02 2013-11-07 Exelixis, Inc. A dual met - vegf modulator for treating osteolytic bone metastases
EP2892532B1 (en) * 2012-09-07 2019-02-13 Exelixis, Inc. Inhibitors of met, vegfr and ret for use in the treatment of lung adenocarcinoma
CN103664776B (en) * 2012-09-26 2016-05-04 正大天晴药业集团股份有限公司 The preparation method of a kind of tyrosine kinase inhibitor and intermediate thereof
GEP20196995B (en) 2013-03-15 2019-07-25 Inc Exelixis Metabolites of n-(4-{[6,7-bis (methyloxy)quinolin-4-yl] oxy}phenyl)-n'-(4-fluorophenyl) cyclopropane-1,1-dicarboxamide
CA2908815A1 (en) * 2013-04-04 2014-10-09 Exelixis, Inc. Drug combinations to treat cancer
EP2981263B1 (en) * 2013-04-04 2022-06-29 Exelixis, Inc. Cabozantinib dosage form and use in the treatment of cancer
CN104109124B (en) * 2013-04-19 2016-08-31 正大天晴药业集团股份有限公司 The rich crystal for Buddhist nun 0.5 malate of card
CN104370811B (en) * 2013-08-15 2019-02-12 广东东阳光药业有限公司 A kind of novel crystal forms of quinoline compound and preparation method thereof
CN104649969B (en) * 2013-11-22 2019-02-12 广东东阳光药业有限公司 A kind of salt and preparation method thereof for Buddhist nun's class drug
EP3738952A1 (en) * 2014-02-14 2020-11-18 Exelixis, Inc. Crystalline solid forms of n-{4-[(6,7-dimethoxyquinolin-4-yl)oxy]phenyl}-n'-(4-fluorophenyl) cyclopropane-1,1-dicarboxamide, processes for making, and methods of use
US10159666B2 (en) 2014-03-17 2018-12-25 Exelixis, Inc. Dosing of cabozantinib formulations
MX2016013600A (en) * 2014-04-25 2017-04-27 Exelixis Inc Method of treating lung adenocarcinoma.
EP3145913A1 (en) 2014-05-23 2017-03-29 Mylan Laboratories Ltd. Novel polymorphs of cabozantinib (s)-malate and cabozantinib free base
CN104788372B (en) * 2014-07-25 2018-01-30 上海圣考医药科技有限公司 A kind of deuterated card is rich to replace Buddhist nun's derivative, its preparation method, application and its intermediate
EP3174854B1 (en) 2014-07-31 2022-08-24 Exelixis, Inc. Method of preparing fluorine-18 labeled cabozantinib and its analogs
MX2017001490A (en) 2014-08-05 2017-05-11 Exelixis Inc Drug combinations to treat multiple myeloma.
CN105503717A (en) * 2014-09-24 2016-04-20 江苏奥赛康药业股份有限公司 Cabozantinib malate compound and medicine composition therewith
CN104961680B (en) * 2014-11-07 2017-09-12 苏州晶云药物科技有限公司 The hydrochloride and its polymorphic of the diformamide of N (4 { [6,7 pairs of bases of (methyl epoxide) quinoline 4] epoxide } phenyl) N ' (4 fluorophenyl) cyclopropane 1,1
CN104961681B (en) * 2014-11-13 2017-06-13 苏州晶云药物科技有限公司 The rich mucate and its crystal formation for Buddhist nun of card
EP3274332B1 (en) 2015-03-25 2018-12-19 Sandoz AG Crystalline forms of cabozantinib phosphate and cabozantinib hydrochloride
US10206916B2 (en) 2015-03-25 2019-02-19 Sandoz Ag Cabozantinib salts and their use as anti-cancer agents
EP3337786B1 (en) 2015-08-19 2019-12-11 Sandoz AG Asymmetric bisamidation of malonic ester derivatives
US11141413B2 (en) * 2016-04-15 2021-10-12 Exelixis, Inc. Method of treating renal cell carcinoma using N-(4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, (2S)-hydroxybutanedioate
CN109922790B (en) 2016-09-12 2022-06-14 珠海贝海生物技术有限公司 Cabotinib formulations
KR101829706B1 (en) 2016-09-21 2018-02-19 씨제이헬스케어 주식회사 Acid addition salts of (S)-4-(5,7-difluorochroman-4-yloxy)-N,N,2-trimethyl-1H-benzo[d]imidazole-6-carboxamide
BR112019015011A2 (en) 2017-01-20 2020-04-28 Exelixis Inc combinations of cabozantinib and atezolizumab to treat cancer
CN108341773A (en) * 2017-01-21 2018-07-31 南京华威医药科技开发有限公司 The rich crystal form II for Buddhist nun's malate of card
US11279675B2 (en) * 2017-05-26 2022-03-22 Exelixis, Inc. Crystalline solid forms of salts of N-{4-[(6,7-dimethoxyquinolin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl) cyclopropane-1, 1-dicarboxamide, processes for making, and methods of use
EP3634413A1 (en) * 2017-06-09 2020-04-15 Exelixis, Inc. Liquid dosage forms to treat cancer
CN109836382B (en) * 2017-11-29 2021-11-05 江苏豪森药业集团有限公司 Preparation method of cabozantinib malate and intermediate thereof
CR20200358A (en) 2018-01-26 2021-02-22 Exelixis Inc Compounds for the treatment of kinase-dependent disorders
US11498902B2 (en) * 2018-06-05 2022-11-15 Natco Pharma Limited Process for the preparation of Cabozantinib and its pharmaceutically acceptable salts thereof
JP7409696B2 (en) 2018-06-15 2024-01-09 ハンダ ファーマシューティカルズ インコーポレイテッド Kinase inhibitor salts and compositions thereof
WO2020075196A1 (en) 2018-10-11 2020-04-16 Cipla Limited Polymorphs of n-(4-(6,7-dimethoxyquinolin-4-yloxy) phenyl)-n'-(4-fluorophenyl)cyclopropane-1, 1-dicarboxamide, (s)- malate, methods of production and pharmaceutical uses thereof
WO2021209940A1 (en) * 2020-04-14 2021-10-21 Msn Laboratories Private Limited, R&D Center Pharmaceutical composition containing n-(4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, (2s)-hydroxybutanedioate
IT202000027678A1 (en) 2020-11-18 2022-05-18 Indena Spa CABOZANTINIB-(S)-MALATO AMORPHOUS SOLID DISPERSIONS AND PROCESSES FOR THEIR PREPARATION
CA3202761A1 (en) 2020-11-25 2022-06-02 Nanocopoeia, Llc Amorphous cabozantinib particles and uses thereof
US11590122B2 (en) 2021-02-19 2023-02-28 Slayback Pharma Llc Pharmaceutical compositions of cabozantinib
CA3213086A1 (en) * 2021-03-24 2022-09-29 Ramakrishna Parameshwar Bhat Process for preparation of cabozantinib
CN115215797B (en) * 2021-04-15 2024-04-12 成都苑东生物制药股份有限公司 Novel crystal form of cabozitinib malate and preparation method thereof
WO2023098853A1 (en) * 2021-12-03 2023-06-08 湖南湘源美东医药科技有限公司 Cocrystal of cabozantinib, preparation method therefor and application thereof as drug or in pharmaceutical preparation
WO2023165948A1 (en) 2022-03-01 2023-09-07 Synthon B.V. Cabozantinib salt with l-(+)-tartaric acid and solid forms thereof
WO2023222946A1 (en) 2022-05-18 2023-11-23 Fermion Oy Process for the preparation of cabozantinib
US11814356B1 (en) 2023-03-29 2023-11-14 Apotex Inc. Salt of cabozantinib

Family Cites Families (206)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2160201B (en) 1984-06-14 1988-05-11 Wyeth John & Brother Ltd Quinazoline and cinnoline derivatives
US5123951A (en) 1986-03-31 1992-06-23 Rhone-Poulenc Nederland B.V. Synergistic plant growth regulator compositions
JPS646261A (en) 1987-03-31 1989-01-10 Nisshin Flour Milling Co 4-thioquinazoline derivative, its production and antiulcer agent containing said derivative as active component
US5143854A (en) 1989-06-07 1992-09-01 Affymax Technologies N.V. Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
US5034393A (en) 1989-07-27 1991-07-23 Dowelanco Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives
US5238951A (en) 1991-02-01 1993-08-24 E. R. Squibb & Sons, Inc. Heterocyclic amido prostaglandin analogs
DE4114733A1 (en) 1991-05-06 1992-11-12 Huels Chemische Werke Ag METHOD FOR PRODUCING SUBSTITUTED MALONESTERANILIDES AND MALONIC ACID MONOANILIDES
US5710158A (en) 1991-05-10 1998-01-20 Rhone-Poulenc Rorer Pharmaceuticals Inc. Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
US5480883A (en) 1991-05-10 1996-01-02 Rhone-Poulenc Rorer Pharmaceuticals Inc. Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
US6057344A (en) 1991-11-26 2000-05-02 Sepracor, Inc. Methods for treating hypertension, and angina using optically pure (-) amlodipine
US6498144B1 (en) 1993-10-18 2002-12-24 North Shore - Long Island Jewish Research Institute Use of scatter factor to enhance angiogenesis
IL112249A (en) 1994-01-25 2001-11-25 Warner Lambert Co Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
GB9510757D0 (en) 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
TW321649B (en) 1994-11-12 1997-12-01 Zeneca Ltd
GB9508538D0 (en) 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
US5747498A (en) 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
DK0831829T3 (en) 1995-06-07 2003-12-15 Pfizer Heterocyclic, ring-condensed pyrimidine derivatives
DE69618587T2 (en) 1995-06-07 2002-08-29 Sugen Inc CHINAZOLINE AND PHARMACEUTICAL COMPOSITIONS
US5650415A (en) 1995-06-07 1997-07-22 Sugen, Inc. Quinoline compounds
GB9514265D0 (en) 1995-07-13 1995-09-13 Wellcome Found Hetrocyclic compounds
EP0860433B1 (en) 1995-11-07 2002-07-03 Kirin Beer Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of growth factor receptor originating in platelet and pharmaceutical compositions containing the same
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
NZ325248A (en) 1995-12-23 1999-09-29 Pfizer Res & Dev Quinoline and quinazoline compounds useful in therapy
SK285141B6 (en) 1996-02-13 2006-07-07 Astrazeneca Uk Limited Use of quinazoline derivative, quinazoline derivative, process for preparation thereof and pharmaceutical composition containing thereof
GB9603095D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
KR100489174B1 (en) 1996-03-05 2005-09-30 제네카-파마 소시에떼아노님 4-anilinoquinazoline derivatives
DE69734149T2 (en) 1996-03-15 2006-07-06 Astrazeneca Ab CINOLINE DERIVATIVES AND USE AS CEREALS
US6107300A (en) 1996-03-27 2000-08-22 Dupont Pharmaceuticals Arylamino fused pyrimidines
DK0892789T4 (en) 1996-04-12 2010-04-06 Warner Lambert Co Irreversible inhibitors of tyrosine kinases
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
ID19609A (en) 1996-07-13 1998-07-23 Glaxo Group Ltd HETEROSICLIC COMPOUNDS
US5962407A (en) 1996-07-26 1999-10-05 Kelly; Michael T. Loloatin derivatives and analogs
AU733551B2 (en) 1996-09-25 2001-05-17 Astrazeneca Ab Qinoline derivatives inhibiting the effect of growth factors such as VEGF
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
ATE480521T1 (en) 1996-10-01 2010-09-15 Kyowa Hakko Kirin Co Ltd NITROGEN CONTAINING HETEROCYCLIC COMPOUNDS
GB9700504D0 (en) 1997-01-11 1997-02-26 Pfizer Ltd Pharmaceutical compounds
GB9705361D0 (en) 1997-03-14 1997-04-30 Celltech Therapeutics Ltd Chemical compounds
UA73073C2 (en) 1997-04-03 2005-06-15 Уайт Холдінгз Корпорейшн Substituted 3-cyan chinolines
ATE244225T1 (en) 1997-04-18 2003-07-15 Kirin Brewery METHOD FOR PRODUCING QUINOLINE DERIVATIVES
ES2207834T3 (en) 1997-04-22 2004-06-01 Janssen Pharmaceutica N.V. QUINO- AND ANTAGONIST QUINAZOLINS OF CRF.
GB9708917D0 (en) 1997-05-01 1997-06-25 Pfizer Ltd Compounds useful in therapy
AR012634A1 (en) 1997-05-02 2000-11-08 Sugen Inc QUINAZOLINE BASED COMPOUND, FAMACEUTICAL COMPOSITION THAT UNDERSTANDS IT, METHOD TO SYNTHESIZE IT, ITS USE, METHODS OF MODULATION OF THE DESERINE / TREONIN PROTEIN-KINASE FUNCTION AND IN VITRO METHOD TO IDENTIFY COMPOUNDS THAT MODULATE
ZA986732B (en) 1997-07-29 1999-02-02 Warner Lambert Co Irreversible inhibitiors of tyrosine kinases
AU8816298A (en) 1997-08-22 1999-03-16 Zeneca Limited Oxindolylquinazoline derivatives as angiogenesis inhibitors
RS49779B (en) 1998-01-12 2008-06-05 Glaxo Group Limited, Byciclic heteroaromatic compounds as protein tyrosine kinase inhibitors
AU4317399A (en) 1998-05-28 1999-12-13 Parker Hughes Institute Quinazolines for treating brain tumor
AU5620299A (en) 1998-08-11 2000-03-06 Novartis Ag Isoquinoline derivatives with angiogenesis inhibiting activity
KR20010089171A (en) 1998-08-21 2001-09-29 추후제출 Quinazoline derivatives
US6184226B1 (en) 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
WO2000015202A2 (en) 1998-09-10 2000-03-23 Ipr-Institute For Pharmaceutical Research Ag Topical application products
PT1117659E (en) 1998-09-29 2004-04-30 Wyeth Corp SUBSTITUTED CYANOCHINOLINES AS PROTEIN TYROSINE KINASE INHIBITORS
US6288082B1 (en) 1998-09-29 2001-09-11 American Cyanamid Company Substituted 3-cyanoquinolines
US6593333B1 (en) 1998-10-01 2003-07-15 Astrazeneca Ab Substituted anilino-quinazoline (or quinoline) compounds and use thereof
FR2784030B1 (en) 1998-10-02 2002-12-20 Inst Nat Sante Rech Med USE OF CALCIUM AND / OR CGMP-DEPENDENT CHANNEL BLOCKERS FOR THE TREATMENT OF RETINE CONDITIONS
CN1161352C (en) 1998-10-08 2004-08-11 阿斯特拉曾尼卡有限公司 Quinazoline derivatives
EA003786B1 (en) 1998-11-19 2003-10-30 Варнер Ламберт Компани N-[4-(3-chloro-4-fluoro-phenylamino)-7-(3-morpholin-4-yl-propoxy)-quinazolin-6-yl]-acrylamide, an irreversible inhibitor of tyrosine kinases
JP3519368B2 (en) 1999-01-22 2004-04-12 麒麟麦酒株式会社 Quinoline derivatives and quinazoline derivatives
HU228964B1 (en) 1999-02-10 2013-07-29 Astrazeneca Ab Quinazoline derivatives as angiogenesis inhibitors, process for their preparation and medicaments containing them
GB9904103D0 (en) 1999-02-24 1999-04-14 Zeneca Ltd Quinoline derivatives
US6080747A (en) 1999-03-05 2000-06-27 Hughes Institute JAK-3 inhibitors for treating allergic disorders
DE19911509A1 (en) 1999-03-15 2000-09-21 Boehringer Ingelheim Pharma Bicyclic heterocycles, medicaments containing these compounds, their use and processes for their preparation
US6258820B1 (en) 1999-03-19 2001-07-10 Parker Hughes Institute Synthesis and anti-tumor activity of 6,7-dialkoxy-4-phenylamino-quinazolines
WO2000056338A1 (en) 1999-03-19 2000-09-28 Parker Hughes Institute Quinazoline formulations and therapeutic use thereof
CA2368647A1 (en) 1999-03-31 2000-10-05 The Procter & Gamble Company Viral treatment
YU13200A (en) 1999-03-31 2002-10-18 Pfizer Products Inc. Process and intermediates for preparing anti-cancer compounds
GB9910580D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
GB9910577D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
US6126917A (en) 1999-06-01 2000-10-03 Hadasit Medical Research Services And Development Ltd. Epidermal growth factor receptor binding compounds for positron emission tomography
KR100709909B1 (en) 1999-06-21 2007-04-24 베링거 잉겔하임 파르마 게엠베하 운트 코 카게 Bicyclic heterocycles, medicaments containing these compounds and methods for the production thereof
GB9922171D0 (en) 1999-09-21 1999-11-17 Zeneca Ltd Chemical compounds
WO2001021596A1 (en) 1999-09-21 2001-03-29 Astrazeneca Ab Quinazoline derivatives and their use as pharmaceuticals
US6759410B1 (en) 1999-11-23 2004-07-06 Smithline Beecham Corporation 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors
CA2392554A1 (en) 1999-11-30 2001-06-28 Parker Hughes Institute Inhibitors of thrombin induced platelet aggregation
US20020002169A1 (en) 1999-12-08 2002-01-03 Griffin John H. Protein kinase inhibitors
US7135466B2 (en) 1999-12-24 2006-11-14 Kirin Beer Kabushiki Kaisha Quinoline and quinazoline derivatives and drugs containing the same
US6525046B1 (en) 2000-01-18 2003-02-25 Boehringer Ingelheim Pharmaceuticals, Inc. Aromatic heterocyclic compounds as antiinflammatory agents
US6977259B2 (en) 2000-01-28 2005-12-20 Astrazeneca Ab Quinoline derivatives and their use as aurora 2 kinase inhibitors
US6664390B2 (en) 2000-02-02 2003-12-16 Warner-Lambert Company Llc Method for the simplified production of (3-chloro-4-fluorophenyl)-[7-(3-morpholin-4-yl-propoxy)-6-nitro-quinazoline-4-yl]-amine or (3-chloro-4-fluorophenyl)-[7-(3-morpholin-4-yl-propoxy)-6-amino-quinazoline-4-yl]-amine
SK12712002A3 (en) 2000-02-07 2003-02-04 Abbott Gmbh & Co. Kg 2-Benzothiazolyl urea derivatives and their use as protein kinase inhibitors
CN1329390C (en) 2000-02-15 2007-08-01 苏根公司 Pyrrole substituted 2-indolinone protein kinase inhibitors
EA200200976A1 (en) 2000-03-13 2003-02-27 Американ Цианамид Компани METHOD FOR THE TREATMENT OR INHIBITION OF POLYPIC POLYPES
US6521618B2 (en) 2000-03-28 2003-02-18 Wyeth 3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
US6608048B2 (en) 2000-03-28 2003-08-19 Wyeth Holdings Tricyclic protein kinase inhibitors
US6627634B2 (en) 2000-04-08 2003-09-30 Boehringer Ingelheim Pharma Kg Bicyclic heterocycles, pharmaceutical compositions containing them, their use, and processes for preparing them
UA73993C2 (en) 2000-06-06 2005-10-17 Астразенека Аб Quinazoline derivatives for the treatment of tumours and a pharmaceutical composition
MXPA02012870A (en) 2000-06-22 2003-05-14 Pfizer Prod Inc Substituted bicyclic derivatives for the treatment of abnormal cell growth.
EP1174118A1 (en) 2000-06-28 2002-01-23 Cognis France S.A. Use of inulin and derivatives thereof
EE200200715A (en) 2000-06-28 2004-08-16 Astrazeneca Ab Substituted quinazoline derivatives and their use as inhibitors
FR2811658B1 (en) 2000-07-17 2004-07-02 Cfpi Nufarm BIOLOGICAL REACTOR WITH SUBMERGED FIXED BED AND METHOD FOR TREATING LIQUID EFFLUENTS
JP2002030083A (en) * 2000-07-18 2002-01-29 Kirin Brewery Co Ltd N-(2-chloro-4-{[6-methoxy-7-(3-pyridylmethoxy)-4- quinolyl]oxy}phenyl)-n'-propylurea dihydrochloride
CA2417500C (en) 2000-07-28 2008-11-18 Georgetown University Medical Center Erbb-2 selective small molecule kinase inhibitors
RU2267489C2 (en) 2000-08-21 2006-01-10 Астразенека Аб Quinazoline derivatives, method for their preparing and pharmaceutical composition
FR2813307B1 (en) 2000-08-23 2002-11-08 Sanofi Synthelabo AMINOALKENYLBENZOYL-BENZOFURANS OR BENZOTHIOPHENES, PROCESS FOR THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM
US6653305B2 (en) 2000-08-26 2003-11-25 Boehringer Ingelheim Pharma Kg Bicyclic heterocycles, pharmaceutical compositions containing them, their use, and processes for preparing them
US6403580B1 (en) 2000-08-26 2002-06-11 Boehringer Ingelheim Pharma Kg Quinazolines, pharmaceutical compositions containing these compounds, their use and processes for preparing them
US6740651B2 (en) 2000-08-26 2004-05-25 Boehringer Ingelheim Pharma Kg Aminoquinazolines which inhibit signal transduction mediated by tyrosine kinases
US6617329B2 (en) 2000-08-26 2003-09-09 Boehringer Ingelheim Pharma Kg Aminoquinazolines and their use as medicaments
DE10042058A1 (en) 2000-08-26 2002-03-07 Boehringer Ingelheim Pharma Bicyclic heterocycles, medicaments containing these compounds, their use and processes for their preparation
US6656946B2 (en) 2000-08-26 2003-12-02 Boehringer Ingelheim Pharma Kg Aminoquinazolines which inhibit signal transduction mediated by tyrosine kinases
AU2001292138A1 (en) 2000-10-13 2002-04-22 Astrazeneca Ab Quinazoline derivatives with anti-tumour activity
US6939866B2 (en) 2000-10-13 2005-09-06 Astrazeneca Ab Quinazoline derivatives
ES2318649T3 (en) 2000-10-20 2009-05-01 EISAI R&D MANAGEMENT CO., LTD. PROCEDURE FOR PREPARATION OF DERIVATIVES OF 4-FENOXI QUINOLINAS.
JP2004512335A (en) 2000-10-25 2004-04-22 アストラゼネカ アクチボラグ Quinazoline derivatives
WO2002036577A1 (en) 2000-11-02 2002-05-10 Nippon Shinyaku Co., Ltd. Quinazoline derivatives and drugs
EP1337513A1 (en) 2000-11-02 2003-08-27 AstraZeneca AB 4-substituted quinolines as antitumor agents
EP1337524A1 (en) 2000-11-02 2003-08-27 AstraZeneca AB Substituted quinolines as antitumor agents
US7019012B2 (en) 2000-12-20 2006-03-28 Boehringer Ingelheim International Pharma Gmbh & Co. Kg Quinazoline derivatives and pharmaceutical compositions containing them
US6900220B2 (en) 2001-01-02 2005-05-31 Syntex (U.S.A.) Llc Quinazolone derivatives as alpha 1A/B adrenergic receptor antagonists
GB0103046D0 (en) 2001-02-07 2001-03-21 Novartis Ag Organic Compounds
JP2002265365A (en) 2001-03-08 2002-09-18 Koyo Chemical Kk Neutrophil function inhibitor
DE60229046D1 (en) 2001-04-19 2008-11-06 Astrazeneca Ab CHINAZOLINE DERIVATIVES
WO2002088110A1 (en) 2001-04-27 2002-11-07 Kirin Beer Kabushiki Kaisha Quinoline derivative having azolyl group and quinazoline derivative
SE0101675D0 (en) 2001-05-11 2001-05-11 Astrazeneca Ab Novel composition
WO2002092577A1 (en) 2001-05-14 2002-11-21 Astrazeneca Ab Quinazoline derivatives
WO2002092578A1 (en) 2001-05-14 2002-11-21 Astrazeneca Ab Quinazoline derivatives
WO2002092579A1 (en) 2001-05-14 2002-11-21 Astrazeneca Ab 4-anilinoquinazoline derivatives
US6734303B2 (en) 2001-05-18 2004-05-11 Pfizer Inc. Process for the production of quinazolines
DE10125432A1 (en) 2001-05-25 2002-11-28 Bayer Ag New benzoyl-substituted aliphatic ketones or aldehydes, useful as herbicides or fungicides, especially as pre- and post-emergence selective herbicides against a broad spectrum of weeds
AU2002350105A1 (en) 2001-06-21 2003-01-08 Ariad Pharmaceuticals, Inc. Novel quinazolines and uses thereof
KR100883731B1 (en) 2001-06-22 2009-02-12 기린 파마 가부시끼가이샤 Quinoline Derivative and Quinazoline Derivative Inhibiting Self-Phosphorylation of Hepatocytus Proliferator Receptor, and Medicinal Composition Containing the Same
KR100397792B1 (en) 2001-06-28 2003-09-13 한국과학기술연구원 4-(phenylamino)-[1,4]dioxano[2,3-g]quinazoline Derivatives and Process for Preparing the Same
GB0118752D0 (en) 2001-08-01 2001-09-26 Pfizer Ltd Process for the production of quinazolines
US7229774B2 (en) 2001-08-02 2007-06-12 Regents Of The University Of Michigan Expression profile of prostate cancer
ES2453164T3 (en) 2001-08-15 2014-04-04 Pharmacia & Upjohn Company Llc Crystals including a malic acid salt of N- [2- (diethylamino) ethyl] -5 - [(5-fluoro-1,2-dihydro-2-oxo-3H-indole-3-ylidene) methyl] -2 , 4-dimethyl-1H-pyrrole-3-carboxamide, processes for its preparation and its compositions
US20030066060A1 (en) 2001-09-28 2003-04-03 Ford Richard L. Cross profile guided optimization of program execution
WO2003033472A1 (en) 2001-10-17 2003-04-24 Kirin Beer Kabushiki Kaisha Quinoline or quinazoline derivatives inhibiting auto- phosphorylation of fibroblast growth factor receptors
AU2002361577A1 (en) 2001-10-30 2003-05-12 Merck And Co., Inc. Tyrosine kinase inhibitors
GB0126433D0 (en) 2001-11-03 2002-01-02 Astrazeneca Ab Compounds
US7319107B2 (en) 2001-11-08 2008-01-15 Johnson & Johnson Consumer Companies, Inc. 1,2,4-thiadiazolium derivatives as melanocortin receptor modulators
GB0128108D0 (en) 2001-11-23 2002-01-16 Astrazeneca Ab Therapeutic use
PL370137A1 (en) 2001-11-27 2005-05-16 Wyeth Holdings Corporation 3-cyanoquinolines as inhibitors of egf-r and her2 kinases
GB0129099D0 (en) 2001-12-05 2002-01-23 Astrazeneca Ab Chemical compounds
AU2002347359A1 (en) 2001-12-05 2003-06-17 Astrazeneca Ab Quinoline derivatives
WO2003048159A1 (en) 2001-12-05 2003-06-12 Astrazeneca Ab Quinoline derivatives
CA2469730A1 (en) 2001-12-10 2003-06-19 Aryx Therapeutics Novel methods for treatment of cardiac arrhythmia, synthesis, and methods of use
RS46404A (en) 2001-12-12 2006-10-27 Pfizer Products Inc. Salt forms of e-2-methoxy-n-(3-(4-(3-methyul-pyridin-3- yloxy)-phenylamino)-quinazolin-6-yl)-allyl)-acetamide,its preparation and its use against cancer
OA12734A (en) 2001-12-12 2006-06-28 Pfizer Prod Inc Quinazoline derivatives for the treatment of abnormal cell growth.
TW200301123A (en) 2001-12-21 2003-07-01 Astrazeneca Uk Ltd New use
WO2003055866A1 (en) 2001-12-21 2003-07-10 Bayer Pharmaceuticals Corporation Quinazoline and quinoline derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents
CA2471577C (en) 2001-12-24 2011-08-02 Astrazeneca Ab Chemical compounds
EP2181996A1 (en) 2002-01-29 2010-05-05 Glaxo Group Limited Aminopiperidine derivatives
JP4508650B2 (en) 2002-01-29 2010-07-21 グラクソ グループ リミテッド Aminopiperidine compound, process for producing the compound and pharmaceutical composition containing the compound
CA2473572C (en) 2002-02-01 2011-05-10 Astrazeneca Ab Quinazoline compounds
DE10204462A1 (en) 2002-02-05 2003-08-07 Boehringer Ingelheim Pharma Use of tyrosine kinase inhibitors for the treatment of inflammatory processes
TW200813014A (en) 2002-03-28 2008-03-16 Astrazeneca Ab Quinazoline derivatives
DE10217689A1 (en) 2002-04-19 2003-11-13 Boehringer Ingelheim Pharma Bicyclic heterocycles, medicaments containing these compounds, their use and processes for their preparation
US6693198B2 (en) 2002-04-22 2004-02-17 Xanthus Life Sciences, Inc. Amonafide salts
AU2003235838A1 (en) 2002-05-01 2003-11-17 Kirin Beer Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of macrophage colony stimulating factor receptor
US7323479B2 (en) 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
ES2400339T3 (en) 2002-07-15 2013-04-09 Symphony Evolution, Inc. Compounds, pharmaceutical compositions thereof and their use in the treatment of cancer
GB0219746D0 (en) 2002-08-23 2002-10-02 Inst Of Ex Botany Ascr Azapurine derivatives
AU2003257666A1 (en) 2002-08-23 2004-03-11 Kirin Beer Kabushiki Kaisha COMPOUND HAVING TGFss INHIBITORY ACTIVITY AND MEDICINAL COMPOSITION CONTAINING THE SAME
US7419984B2 (en) 2002-10-17 2008-09-02 Cell Therapeutics, Inc. Pyrimidines and uses thereof
DE60316590T2 (en) 2002-10-21 2008-06-19 Kirin Beer K.K. N- (2-CHLORO-4 - ((6,7-DIMETHOXY-4-CHINOLYL) OXYPHENYL-N '- (5-METHYL-3-ISOXAZOLYL) UREA SALT IN CRYSTALLINE FORM
EP1566379A4 (en) 2002-10-29 2005-11-09 Kirin Brewery QUINOLINE DERIVATIVES AND QUINAZOLINE DERIVATIVES INHIBITING AUTOPHOSPHORYLATION OF Flt3 AND MEDICINAL COMPOSITIONS CONTAINING THE SAME
US7462623B2 (en) 2002-11-04 2008-12-09 Astrazeneca Ab Quinazoline derivatives as Src tyrosine kinase inhibitors
WO2004055003A1 (en) 2002-12-13 2004-07-01 Neurogen Corporation 2-substituted quinazolin-4-ylamine analogues as capsaicin receptor modulators
RU2005119172A (en) 2002-12-18 2006-01-20 Пфайзер Продактс Инк. (Us) 4-ANILINKHINAZOLINE DERIVATIVES FOR TREATMENT OF PATHOLOGICAL CELL GROWTH
WO2004058267A1 (en) 2002-12-23 2004-07-15 Ariad Pharmaceuticals, Inc. Heterocycles and uses thereof
AU2003292838A1 (en) 2002-12-27 2004-07-29 Kirin Beer Kabushiki Kaisha Therapeutic agent for wet age-related macular degeneration
US8176532B1 (en) 2003-03-17 2012-05-08 Sprint Communications Company L.P. Secure access point for scada devices
AU2004221812B2 (en) 2003-03-19 2010-02-18 Exelixis Inc. Tie-2 modulators and methods of use
KR100559180B1 (en) 2003-05-20 2006-03-14 김민서 Electronic settlement method and server according to conditional trade
WO2005003140A1 (en) 2003-07-02 2005-01-13 Pharmacia & Upjohn Company Llc 4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamides as antiviral agents
US20070213374A1 (en) 2003-07-07 2007-09-13 Merck Patent Gmbh Malonamide Derivatives
JP4299090B2 (en) * 2003-09-24 2009-07-22 株式会社東海理化電機製作所 Operation device for vehicle air conditioner
JP4638436B2 (en) 2003-09-26 2011-02-23 エグゼリクシス, インコーポレイテッド c-Met modulators and uses thereof
EA012621B1 (en) 2003-11-07 2009-10-30 Чирон Корпорейшн Pharmaceutically acceptable salts of quinolinone compounds having improved pharmaceutical properties
CN101337931B (en) 2003-12-25 2010-09-29 卫材R&D管理有限公司 Crystal of salt of 4-(3-chloro-4-(cyclopropylaminocarbonyl)amino-phenoxy)-7-methoxy-6-quinolinecarboxamide or of solvate thereof and processes for producing these
EP1711495A2 (en) 2004-01-23 2006-10-18 Amgen Inc. Quinoline, quinazoline, pyridine and pyrimidine counds and their use in the treatment of inflammation, angiogenesis and cancer
MY144177A (en) 2004-02-04 2011-08-15 Novartis Ag Salt forms of 4-(4-methylpiperazin-1-ylmethyl)-n-[4-methyl-3-(4-pyridin-3-yl)pyrimidin-2-ylamino)phenyl]-benzamide.
US20060035940A1 (en) 2004-03-16 2006-02-16 Sepracor Inc. (S)-Amlodipine malate
US7173031B2 (en) 2004-06-28 2007-02-06 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
CA2572331A1 (en) * 2004-07-02 2006-02-09 Exelixis, Inc. C-met modulators and method of use
US20060197914A1 (en) * 2005-03-04 2006-09-07 Colorlink, Inc. Four panel projection system
JP2008537748A (en) 2005-04-06 2008-09-25 エクセリクシス、インコーポレイテッド c-Met Modulator and Method of Use
US20080298657A1 (en) 2005-11-23 2008-12-04 Junji Shiraishi Computer-Aided Method for Detection of Interval Changes in Successive Whole-Body Bone Scans and Related Computer Program Program Product and System
WO2007102074A2 (en) 2006-03-07 2007-09-13 Cadila Healthcare Limited Salts of quetiapine
JP2009529047A (en) 2006-03-07 2009-08-13 アレイ バイオファーマ、インコーポレイテッド Heterobicyclic pyrazole compounds and uses thereof
US20080027223A1 (en) 2006-03-23 2008-01-31 Teva Pharmaceutical Industries Ltd. Polymorphs of eszopiclone malate
US20080004273A1 (en) 2006-05-30 2008-01-03 Stephane Raeppel Inhibitors of protein tyrosine kinase activity
JP5190365B2 (en) 2006-08-23 2013-04-24 エーザイ・アール・アンド・ディー・マネジメント株式会社 Salt of phenoxypyridine derivative or crystal thereof and method for producing the same
WO2008070616A2 (en) 2006-12-01 2008-06-12 University Of Utah Research Foundation METHODS AND COMPOSITIONS RELATED TO HIF-1α
CN101605540A (en) 2006-12-14 2009-12-16 埃克塞利希斯股份有限公司 Use the method for mek inhibitor
WO2008083319A1 (en) 2006-12-29 2008-07-10 Il Yang Pharmaceutical Company, Ltd. Solid state forms of enantiopure ilaprazole
CA2812705C (en) 2007-12-19 2015-08-18 Sunovion Pharmaceuticals Inc. Maleate, besylate and l-malate salts of 6-(5-chloro-2-pyridyl)-5-[(4-methyl-1-piperazinyl)carbonyloxy]-7-oxo-6,7-dihydro-5h-pyrrolo[3,4-b]pyrazine
UY31800A (en) 2008-05-05 2009-11-10 Smithkline Beckman Corp CANCER TREATMENT METHOD USING A CMET AND AXL INHIBITOR AND AN ERBB INHIBITOR
AR075084A1 (en) 2008-09-26 2011-03-09 Smithkline Beecham Corp PREPARATION METHOD OF QUINOLINIL -OXIDIFENIL - CYCLOPROPANODICARBOXAMIDS AND CORRESPONDING INTERMEDIARIES
EP2349328A1 (en) 2008-10-01 2011-08-03 Ludwig Institute For Cancer Research Methods for the treatment of cancer
AU2009313970A1 (en) 2008-11-13 2010-05-20 Exelixis Inc. Methods of preparing quinoline derivatives
TW201028383A (en) 2008-12-04 2010-08-01 Exelixis Inc Methods of preparing quinoline derivatives
TWI577664B (en) * 2009-01-16 2017-04-11 艾克塞里克斯公司 Malate salt of n-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, pharmaceutical composition comprising the same and use thereof
MX2012000809A (en) 2009-07-17 2012-03-14 Exelixis Inc Crystalline forms of n-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholi n-4-ylpropyl)oxy]-quinolin-4-yl}oxy)phenyl]-n'-(4-fluorophenyl)c yclopropane-1, 1-dicarboxamide.
UA108618C2 (en) 2009-08-07 2015-05-25 APPLICATION OF C-MET-MODULATORS IN COMBINATION WITH THEMOSOLOMID AND / OR RADIATION THERAPY FOR CANCER TREATMENT
WO2011031840A1 (en) 2009-09-09 2011-03-17 Quintiles Transnational Corp. Methods and compositions for the treatment of receptor tyrosine kinase mediated diseases or disorders
CN102933551A (en) 2010-03-12 2013-02-13 埃克塞里艾克西斯公司 Hydrated crystalline forms of n-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]-quinolin-4-yl}oxy)phenyl]-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
US20120070368A1 (en) 2010-04-16 2012-03-22 Exelixis, Inc. Methods of Using C-Met Modulators
US9724342B2 (en) 2010-07-16 2017-08-08 Exelixis, Inc. C-met modulator pharmaceutical compositions
US9717720B2 (en) 2011-02-10 2017-08-01 Exelixis, Inc. Processes for preparing quinoline compounds and pharmaceutical compositions containing such compounds
US20120252840A1 (en) 2011-04-04 2012-10-04 Exelixis, Inc. Method of Treating Cancer
CA2848512A1 (en) 2011-09-22 2013-03-28 Exelixis, Inc. Method for treating osteoporosis
WO2013166296A1 (en) 2012-05-02 2013-11-07 Exelixis, Inc. A dual met - vegf modulator for treating osteolytic bone metastases
EP2892532B1 (en) 2012-09-07 2019-02-13 Exelixis, Inc. Inhibitors of met, vegfr and ret for use in the treatment of lung adenocarcinoma
CA2908815A1 (en) 2013-04-04 2014-10-09 Exelixis, Inc. Drug combinations to treat cancer
US10159666B2 (en) 2014-03-17 2018-12-25 Exelixis, Inc. Dosing of cabozantinib formulations

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